| Tag | Content |
|---|
EnhancerAtlas ID | HS118-04909 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr12:114917690-114919150 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RARA | MA0729.1 | chr12:114918270-114918288 | CCTTAACCTTTTCACCCT | - | 6.11 | | ZNF263 | MA0528.1 | chr12:114918162-114918183 | GGAGGAGGAGGAAGGGGAGGG | + | 10.33 | | ZNF263 | MA0528.1 | chr12:114918159-114918180 | GGAGGAGGAGGAGGAAGGGGA | + | 10.49 | | ZNF263 | MA0528.1 | chr12:114918165-114918186 | GGAGGAGGAAGGGGAGGGAGA | + | 10.62 | | ZNF263 | MA0528.1 | chr12:114918153-114918174 | GGGTGAGGAGGAGGAGGAGGA | + | 8.21 | | ZNF263 | MA0528.1 | chr12:114918156-114918177 | TGAGGAGGAGGAGGAGGAAGG | + | 9.19 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_68365 | chr12:114909192-114920281 | TC32 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH12I114479 | chr12 | 114917384 | 114918204 | | GH12I114481 | chr12 | 114919107 | 114919420 |
|
Enhancer Sequence | GCAGTCTTTT AGGGTCGCCG GACCGGCTTC CTGGAATACC TGAGGTCGCA GATTCAGGTA 60
GTAAACAGAT GTGGGGTCCA CCCTCCGCCA AATGGGCGGG GCAAGTTCAA CATCCCGCCT 120
CCCCGACCTT AAGTGCGCAG GGCGCCTGGT GCTCGCTTGC CGAAAACGTT AAACATTTTT 180
CTTTGATCCC GCTCTTTTTT TGGGGGGAAA AATGTCTGGG GAAGAGGGAA GTAGTGGGGG 240
AGTGAGGTGC CTGCCCAAGC GAAATTTTGA TGCCCGCCTG CCTCTGGCTC CAGCTCCGCC 300
CTCACGGAAG GGGGAGAACT TCGAATTCCA GAACCGGAAT CCTTGCCTAA TTTTTTTTTT 360
TTTTTTTTTT TGAAATTGAT CGATTTTATC CGGGAGCTTC AAATCGAAAC CAGGAGAGAG 420
GCTTTGAAAT GTCAAAGAAA AGCTACGAAA GAAAAAAGGG GTGGGGTGAG GAGGAGGAGG 480
AGGAAGGGGA GGGAGATTAA AAAAATAATA ATAAGGCGGG GAGGCAGGCA GAGGTTTTCT 540
TTCGAAGTGT AATCGCGGCG CTGCGTACCT TTGTAAGGGT CCTTAACCTT TTCACCCTTT 600
TGGTGGTGGC GGTGGTGGGC TCCTCGTAGC TCTTTGAAAA TCTAATGGGA GCTATGGACC 660
GTCTGCCTGG AAAAATGCCC TTTAGGTACA TGCTTGGCGG GAGCCGGGAG TGAAACCGTT 720
TTTTGCGCAA CTTGGGAAAG TTTTTGCAAT ATTCTCTGCT CAGCCATTTG AGTTGGAATG 780
GAACCGTTCC CAATTTTAAT TTTTGAAGAG ACAGTTTTGC CTGGAGTAAT CTAAACCCAT 840
TTTGGCGGGG AGGGGAGGGC GAGGGGAATT TCAAAATTTA TGCCTTCTTC ACCTTCTGGA 900
GAAGGCAAGA TCCGGCAGGC GACGCTGATT AGCTGGGGGT CTCCGATGCG ACCCCGGACT 960
CGGAGCAGGA AATCCTGGGT GCTCCTGAAG CTCCGCCTGC CCCGGGTTCC AGCGAGAGCA 1020
CCTCGTCACA CTCGGGGCGC TGTCCCCCAG TCCTTTTCCT TCTGGACTCC AGGACCTGAG 1080
GCTCCTGCAG CGGAGAGCTG GGGAAGGGGG ATGAGTTCAA AACTATCTCC CTGTCCTTCC 1140
CTTTGAGATA AGGCATCAAC CTGGGAAGAG TCCCGACTGG TGCAGGGAGC TGCCTGTTCA 1200
GGAAGCCCGG GAGATGCAGA TTCGATTGAT TTCAGAGAGC TTCCAGTCTT TTTCCTGCCC 1260
TGGTGCTAAG AGGATCGAAA TACATTTTTT AGGATTCATG GGAAACCTAG TTCTCATTAT 1320
TAAGAGGCTG TTTTGAAGCC CCTCTGATGG CAAGGAGCCC TGGCGCTTGG AGCGAGAAAG 1380
TGGGTGCAGG TCTCTCCAAA GAGAGCTGAG CTCATTCTGC AGCTCCCTTT CCAGCAGTGG 1440
TTCAGGGCTG GCGCTGCAGA 1460
|
